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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1842804Generated: October 31, 2026

2-Pentanol → HCID 71240769, compound

https://huagongshe.com/reaction/1842804

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-PentanolHCID 22386—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant3-(2-Chloro-4-pyrimidinyl)pyrazolo[1,5-a]pyridineHCID 71743080—
Reactant2-methoxy-4-(1-methyl-3,6-dihydro-2H-pyridin-4-yl)-5-nitroanilineHCID 86677325—
SolventDimethylformamideHCID 6228—
ProductHCID 71240769HCID 7124076966%

Reaction Steps

A solution of 3-(2-chloropyrimidin-4-yl)pyrazolo[1,5-a]pyridine (Intermediate 152, 256 mg, 1.00 mmol), p-toluene sulphonic acid monohydrate (271 mg, 1.43 mmol) and 2-methoxy-4-(1-methyl-3,6-dihydro-2H-pyridin-4-yl)-5-nitroaniline (Intermediate 3, 250 mg, 0.95 mmol) and 2-pentanol (12 mL) was heated at reflux for 4 h under an atmosphere of N2. The mixture was then concentrated in vacuo and the residue was dissolved in CH3OH. This solution was purified by ion exchange chromatography, using an SCX column, eluting with 7M methanolic ammonia. Fractions containing the desired product were concentrated in vacuo to give a residue that was dissolved into hot DMF (10 mL). This solution was filtered and concentrated in vacuo to provide a gum that was triturated with CH3CN (10 mL) to give the title compound (285 mg, 66%) as a yellow powder; 1H NMR: 2.36 (5H, s), 2.67 (2H, s), 3.07 (2H, s), 4.02 (3H, s), 5.66 (1H, s), 7.00 (1H, s), 7.12 (1H, t), 7.41 (1H, m), 7.45 (1H, m), 8.45 (2H, t), 8.59 (1H, d), 8.83 (2H, t), 8.90 (1H, s); m/z: ES− M-H− 456.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946235B2
Source datasetuspto-grants-2015_02
ORD IDord-794300b82d464c71973db3d9167ecc01
Source noteuspto-grants-2015_02